CA1220791A - Cementitious composite material with metal aggregate - Google Patents

Cementitious composite material with metal aggregate

Info

Publication number
CA1220791A
CA1220791A CA000457930A CA457930A CA1220791A CA 1220791 A CA1220791 A CA 1220791A CA 000457930 A CA000457930 A CA 000457930A CA 457930 A CA457930 A CA 457930A CA 1220791 A CA1220791 A CA 1220791A
Authority
CA
Canada
Prior art keywords
mixture
stainless steel
portland cement
particles
superplasticizer
Prior art date
Legal status (The legal status is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the status listed.)
Expired
Application number
CA000457930A
Other languages
French (fr)
Inventor
John A. Satkowski
Barry Scheetz
Janine M. Rizer
Carl Gotzmer
Current Assignee (The listed assignees may be inaccurate. Google has not performed a legal analysis and makes no representation or warranty as to the accuracy of the list.)
Research One LP
Original Assignee
Research One LP
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Research One LP filed Critical Research One LP
Application granted granted Critical
Publication of CA1220791A publication Critical patent/CA1220791A/en
Expired legal-status Critical Current

Links

Classifications

    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B28/00Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements
    • C04B28/02Compositions of mortars, concrete or artificial stone, containing inorganic binders or the reaction product of an inorganic and an organic binder, e.g. polycarboxylate cements containing hydraulic cements other than calcium sulfates
    • C04B28/04Portland cements
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B14/00Use of inorganic materials as fillers, e.g. pigments, for mortars, concrete or artificial stone; Treatment of inorganic materials specially adapted to enhance their filling properties in mortars, concrete or artificial stone
    • C04B14/02Granular materials, e.g. microballoons
    • C04B14/34Metals, e.g. ferro-silicon
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2103/00Function or property of ingredients for mortars, concrete or artificial stone
    • C04B2103/30Water reducers, plasticisers, air-entrainers, flow improvers
    • C04B2103/32Superplasticisers
    • CCHEMISTRY; METALLURGY
    • C04CEMENTS; CONCRETE; ARTIFICIAL STONE; CERAMICS; REFRACTORIES
    • C04BLIME, MAGNESIA; SLAG; CEMENTS; COMPOSITIONS THEREOF, e.g. MORTARS, CONCRETE OR LIKE BUILDING MATERIALS; ARTIFICIAL STONE; CERAMICS; REFRACTORIES; TREATMENT OF NATURAL STONE
    • C04B2103/00Function or property of ingredients for mortars, concrete or artificial stone
    • C04B2103/50Defoamers, air detrainers
    • YGENERAL TAGGING OF NEW TECHNOLOGICAL DEVELOPMENTS; GENERAL TAGGING OF CROSS-SECTIONAL TECHNOLOGIES SPANNING OVER SEVERAL SECTIONS OF THE IPC; TECHNICAL SUBJECTS COVERED BY FORMER USPC CROSS-REFERENCE ART COLLECTIONS [XRACs] AND DIGESTS
    • Y02TECHNOLOGIES OR APPLICATIONS FOR MITIGATION OR ADAPTATION AGAINST CLIMATE CHANGE
    • Y02WCLIMATE CHANGE MITIGATION TECHNOLOGIES RELATED TO WASTEWATER TREATMENT OR WASTE MANAGEMENT
    • Y02W30/00Technologies for solid waste management
    • Y02W30/50Reuse, recycling or recovery technologies
    • Y02W30/91Use of waste materials as fillers for mortars or concrete

Abstract

ABSTRACT
A cementitious composite material exhibiting a unique combination of high strength, vacuum integrity and thermal properties. Objects made of the material may be cast from mixtures in which a major constituent is a filler which consists of stainless steel particles of particular shapes and size. The east objects are characterized by the absence of a continuous network of interconnected pores and by the presence of a tobermorite phase in the material.

Description

~2~0791 CEMENTITIOUS COMPOSITE MATERIAL
WITH METAL A~GR~GATE
This invention is directed to a new cementitious composite material exhibiting a unique combination of properties. More particularly, it relates to a composite with unusually high strength, vacuum integrity and thermal properties not found in previously known cementitious composite materials and which may be cast into objects in which such a combination of properties is desired.
~ne object of the invention is to provide a cementitious composition which is capable of sustaining a vacuum and wl~ich is t~lerefore of particular ùtility w~nen cast as an article intended to be used as a mold in a process involving the use of the mold in a vacuum environment.
A further object of the invention is to provide a cementitious composite material which comprises Portland cement and irregularly shaped stainless steel particles as the principal filler.
Another object of the invention is to provide a cementitious composite material which comprises Portland cement and irregula~ly shaped stainless steel particles as the principal filler and which is capable of holding a vacuum.
It has been found that the desired combination of properties is obtained from cement mixtures containing a tobermorite-like gel, and which are characterized by the absence of a continuous network of interconnected macroscopically visible pores.
~he invention will be better understood from the description taken in conjunction with the drawings in which:
FIGURE 1 is a photograph of the irregularly shaped stainless steel particles present in t~e composite of the present invention;

:1220791 FIGURE 2 is a dia~rammatic view of an apparatus for testing the vacuum integrity of the composite material after it has been cast as a block;
FIGURE 3 is a schematic view, partly in section, taken throug~ plane 2-2 of Figure 2, FIGURE 4 is a view similar to Figure 2 except that the vacuum integrity of the test piece is measure~1 through the bottom face of the test ~lock rather than through an edge surface as in Figures 2 and 3; and FIGURE 5 is a schematic view partly in section of the apparatus of Figure 4 taken on ~lane 404.
In the description which follows, t~ere is described once specific formulation of a ma~erial with a unique combination of properties, but it is to be understood that the present description is presented by way of illustration and is not intended to be construed as limiting the invention in any way.
Briefly, the invention is a composite material which is produced from a mixture including the following:
(a) Portland Cement (Preferably API Class H) (b) Chemically Active Silica (Preferably tiny spherical particles of amorphous silica known as condensed silica fume) (c) A Type F Superplasticizer (Preferably Sodium Salt of Formaldehyde Condensate of Naphthalene Beta Sulfonic Acid) (d) An Antifoam Agent (e) ~ Second Silica Filler (f) A Metallic Filler (Preferably Stainless Steel) (g) Water Each of the above will now be described in greater detail.
(a) The Portland Cement While it appears that any of the various grades of Portland Cement which are commercially available are ~ r ~Z20791 suitable for the production of the material of this invention, Type III Portland Cement is preferred and the Portland Cement known as API Class H is particularly preferred. Class H is the coarsest grind of Portland Cements. The Portland Cement component comprises between 20 and 33~ by weight of the mixture, about 24.28~ being particularly preferred.
(b) ~ne Chemically Active Silica The chemically active silic~ used in the mixture which produces the cementitious composite material of this invention is preferably an amorphous, non-crystalline, pozzolanic silicon dioxide and is preferably condensed silica fume.
This condensed silica fume is produced as a by-product in the electric arc furnace production of silicon or silicon alloys such as ferrosilicon. The gases whic'n are evolved during the manufacture of ferrosilicon from quartz, coke and iron ore when they are heated to up to about 2000C contain Si and SiO vapors which form SiO2 when t'ney react with air as they emerge from the furnace. These vapors condence and the very tiny spherical particles which result from condensation of the vapors are almost entirely amorphous silica with 20-25 m2/g surface area. Typically, the particles 25 analyze 85-92% SiO2, up to 3% Fe2O3, 1-3% alkali metal oxides, 1-2% C, and the remainder being small amounts of alumina, lime and magnesia. The particles range from 0.01 to 0.3 micron with about 70% being smaller than 0.1 micron. This material is also described in U.S.
30 Patent 4,321,243 issued March 23, 1982.
This constituent is believed to have pozzolanic properties in the present composition. Although in itself it possesses little or no cementitious value, it will, at ordinary temperatures, in t'ne presence of moisture, chemically react with calcium compounds to form compounds A ~

possessing cementitious properties. Two such possible reactions involving the finely divided silica fume and leading to the production of tobermorite miyht be the following:
5cA2sio4+7sio2+loH2o->>2ca5si6 17 2 5CA3SiO5 13 2 2 5 6 17 2 Furthermore, the use of silica fume in the mixture confers additional ~enefits. Because it is so finely divided, it helps to fill any interstital voids in the mixture and because it is chemically reactive it reacts with any Ca(OH)2 present, or which forms from t'ne hydrolysis of calcium silicates in the Portland Cement, and therefore counteracts the known deleterious effects which are produced when free Ca(OH)2 or free Cao are present in cements.
The amount of condensed silica fume in the mixture should be between 2 and 7% by weight and 3.31~ is a preferred amount.
(c) Superplasticizer To make the final mixture more fluid and to permit better wetting and mixing, a plasticizer is included in the composition, the preferred plasticizer being sold as Mighty 100 or Mighty 150, the active ingredient of which is the sodium salt of formaldehyde condensate of naphthalene beta-sulfonic acid. Mighty 100 is available as a powder. Mighty 150 is available as a liquid. While it is not intended to be bound by any theoretical explanation, it is believed that the superplasticizer affects the zeta potential of t~e mixture and prevents flocculation. It also appears to increase the strength of the product by permitting the use of smaller amounts of water. Other known plasticizers may be used in place of Mighty 100 or Mighty lS0 to disperse the silica fume in the mixture. Amounts between 0.~5 and 1.5%
by weight have proven beneficial and a particularly preferred amount is about .47% by weight.

122079~

(d) Antifoaming Agent -The composite produced from the above admixture is improved by the incorporation of an antifoamin~ agent, Tri-n-butyl phosphate being the preferred additive, the purpose of which is to reduce the amount and size of air pockets created or trapped in the final cementitious composite material which would decrease the physical properties. The amount of antifoam agent in the mixture should be between 0.01 and 0.5~ by weight and 0.01~ by weight is a preferred amount.
(e) Fine Aggregate The mixture also includes a fine aggregate, preferably Minusil. Minusil is a crystalline silica - and consists of finely divided - generally finer than 5 micron size particles of quartz or silica. ~mounts between 5 and 20% by weight have been used with excellent results at 11.82% which is a preferred amount. The Minusil appears to increase the density of the product and to increase the strength.
(f) Stainless Steel Particles An essential constituent of the cementitious composite ~aterial is a metal aggregate which enihances thermal conductivity and increases the density of the product. The preferred metal aggre~ate is a mixture of stainless steel particles which are irre~ular in shape and which are shown in Fi~ure 1 which is a photograph of this material. Mixtures of various sizes of particles have been tried and a mixture of 10/25 mesh (U.S. Standard Sieve Sizes) and 80/100 mesh (U.S. StandarA Sieve Sizes) particles in appropriate proportions has been found to compact well and to produce a composition with optimum strength and thermal characteristics. Mixtures prepared to include 100/200 mesh (U.S. StandarA Sieve Sizes) stainless steel particles were found to be too heavy and did not readily mix uniformly into the mixture nor did lZZ0791 they yield the desired combination of thermal properties.
The preferred stainless steel powders are sold as Ancor 316L by Hoeganaes Corporation and are Type 316 Ni-Cr-Mo stainless steel particles having less than O.03~ C. They have a density of 6.8 g/cm . While a variety of combination5 of stainless steel particles coarser than 100/200 mesh have been found useful, a particular preferred mixture is 10/25 mesh - 34.77~ and 80/100 mesh -18.68%, these being percentages of the total weight of the mixture.
(g) Water Water, preferably distilled water, is the final constituent of the mixture required to produce the high strength compo.site of this invention. In order to obtain a product with the desired properties between 5 and 10% of water is added, the preferred amount being 6.65%.
Table I gives a range of preferred proportions of the severdl ingredients in the mixture from ~t~ich the composite is produced.

(In % by Weight) ~angePreferred Portland Cement 20 to 3324.28 ~ctive Condensed Silica Fume 2 to 7 3.31 Water 5 to 106.66 Superplasticizer 0.25 to l.S0.47 30 Antifoam A~ent 0.01 to 0.50.01 Fine Aggregate 5 to 2511.82 S/S-10/25 Mesh up to 5034.77 S/S-80/100 Mesh up to 3018.68 . . ~

lZZ0791 Preparation of the Mix The mix is prepared generally in accordance with ASTM Procedure C 305 for Mechanical Mixing of Hydraulic ~ements (Part 5) as may be seen from the following example in which the order of addition and proportions are believed to be essential in order to obtain the desired properties.
The mixture was prepared in a mixing bowl equipped with a planetary action paddle mixer ~Hobart mixer - ASTM Standard C-305-80) by adding 169 parts by weight of water containing 12 parts by weight of the superplasticizer and 0.64 parts of Tri-n-butyl Phosphate to a blend of 616 parts Class H Portland Cement to which 300 parts Minusil have been added. Then 84 parts by weight of the chemically active condensed silica fume was added with mixing.
Finally, the metal aggreg~te was added to complete the formulation. The metal aggregate comprises a mixture of two or more different sizes of stainless steel powder. A preferred mixture consists of 882 parts by weight of 10/25 mesh size and 474 parts by weight of 80/100 mesh size which have been mixed together, dry, to produce the metal aggregate. The entire batch is mixed to blend the constituents.
The resulting mixture was placed into a brass mold and permitted to cure in a moist box for 24 hours at room temperature, then it was steam cured at 60 degrees centigrade for twenty four ~lours. The result is a composite which possesses the desired combination of properties described below and which retains these properties after several thermal cycles, as it could encounter in certain uses.
The desired properties include (1) vacuum integrity; (2) a low coefficient of expansion; and (3) adequate mechanical st-ength.

~2Z0 791 Because of the use of the several aggregates with distinctly different shapes and sizes a material is produced which is free of macroscopic pores and exhibits a higher thermal conductivity than the usual cementitious materials.
The vacuum inte~rity of the product was determined by casting a block of the same and measuring its porosity after it had been cured, using the apparatus shown in FIGURES 2 and 3. ~IGU~ES 2 and 3 show schematically the setup for testing the leak rate through the sides of the test piece and through the ~ottom of the test piece respectively.
Shown in Figure 2 is the apparatus for testing the vacuum integrity of a test block cast from the previously described compositions comprising (1) means to confine the test block between members which seal off one or more surfaces of the block and which leave one or more surfaces exposed to the surrounding atmosphere and
(2) means operatively connected to the confining means to apply a vacuum to the block.
In Figures 2 and 3 a test block (10) is shown with apparatus for measuring the leak rate through the four side faces (12) of the block. Before the vacuum plate ~14) is applied to the block, the bottom of block (10) is coated with a thin layer of a silicone rubber composite to seal t~e bottom of the block and a coat (16) of epoxy may be painted over the silicone rubber to further insure that the bottom of the block is sealed. A
silicone sealant (18) is tllen applied to the top of the block as strips along the perimeter of the top surface. A
piece of cloth (20) is then laid on top of the test block, and then vacuum plate (14) is placed on the block. A hose (21) connects a fitting on vacuum plate to a source of vacuum (not shown). Means for measuring the leak rate into the block through the exposed edges are operatively connected to the test apparatus.

~,.

~Z20t79~

Figure 4 and 5 show the apparatus as it i~
modified to test the leak rate through the base of the test block. In these Figures, the edges of the block (10) are sealed with a silicone sealant (30) which is then covered by a tape (32) to insure that the edges are sealed. A piece of cloth (33) is placed on the top of the test block and then the vacuum apparatus (14) comprising a top engaging plate (34) and side engaging plates (36) is placed on the so-prepared test bloc~ (10), so as to enclose all ~ut t'ne bottom surface of the block. Plate (34) is equipped with a fitting (38) which is connected to hose (40) which in turn is connected to a source of vacuum. In this test, the leak rate throu~h t~e bottom surface is measured.

TABLE II
Vacuum Integrity (Torr/Hr/Area) Ordinary Cement/
Sand Mortar This Invention Bottom 120 6 Sides 120 10 The thermal properties of the new material of this invention which were determined by standard tests may be seen from TABLE III below wl~ich sets fortl~ the properties of material which has been cured, steam cured, and then cycled one or more times as follows:

lZ207~1 TABLE III
Thermal Properties Thermal Conductivity:

Temperature Thermal Conductivity C F W/mK BTU IN/HR FT2F
# 1 24 75 2.6~ 18.0 121 250 2.71 1~.8 # 2 24 75 1.90 13.2 121 250 2.51 17.4 204 400 2.5 17.3 315 600 2.31 16.0 121 250 - 2.01 13.9 Specific Heat:

Temperature Specific Heat C F J/k~ C CAL/G C
24 75 7~0 .181 121 250 800 .191 20 204 400 845 .202 280 530 1150 .275 Thermal Expansion:

Tem~erature Total C F Expansion C Coefficient 125 2S7 13.3 x 10-4 13.3 x 10-6 200 392 21.6 x 10-4 12.3 x 10-6 300 575 30.8 x 10 11.2 x 10-T~e mechanical properties are shown in TABLE IV
below.

,~

122079i TABLE I V
Mechanical Properties Density 220 LB/FT3 Compressive Strength* 30,880 psi Tensile Strength* 2,180 psi Flexural Strength* 3,680 psi 5 Day Cure: 24 Hours in 140F, 95~RH, followed by 5 thermal cycles (45 minutes up, 45 minutes residence, 45 minutes down;
RT-400F-RT) '~

Claims (15)

THE EMBODIMENTS OF THE INVENTION IN WHICH AN
EXCLUSIVE PROPERTY OR PRIVILEGE IS CLAIMED ARE DEFINED AS
FOLLOWS:
1. A cementitious composite material which comprises Portland cement and irregularly shaped stainless steel particles as the principal filler.
2. A cementitious composite material which comprises Portland cement and irregularly shaped stainless steel particles as the principal filler and which is capable of holding a vacuum.
3. The material of Claim 2 having a thermal conductivity of between about 13 and about 19 BTU/IN/HR/Ft2/°F, a specific heat of between about 0.18 and 0.28 cal/G/°C and a coefficient of thermal expansion between about 12 and 13.5 x 10-6/°K.
4. A mixture from which objects of a cementitious composite material may be cast, which exhibits high strength and vacuum integrity, said mixture comprising:
a. Portland cement b. chemically active silica fume particles c. a less chemically active siliceous fine aggregate d. a superplasticizer e. an antifoam agent f. an irregularly shaped particulate, and g. water
5. The mixture of Claim 4 in which the constituents are present in the following relative proportions in % by weight of the mixture:
a. Portland cement - 20 - 33%
b. chemically active silica fume - 2 - 7 c. less active fine aggregates - 5 - 25%
d. superplasticizer - 0.01 - 1.5%
e. antifoam agent - 0.01 - 0.5%

f. metallic filler -10/25 mesh stainless steel up to 50°%
80/100 mesh stainless steel up to 30%:
and g. water - 5 - 10%.
6. The mixture of Claim 5 in which the relative proportions are approximately:
a. Portland cement - 24 - 25%
b. chemically active silica fume - 3 - 3.5%
c. less active fine aggregate - 10 - 12%
d. superplasticizer - 0.5%
e. antifoam agent - 0.25%
f. metallic filler -10/25 mesh stainless steel up to 35%
80/100 mesh stainless steel up to 20%;
and g. water - 6 - 7%.
7. The mixture of Claim 6 in which the relative proportions are approximately:
a. Portland cement - 24.28%
b. chemically active silica fume - 3.31%
c. less active fine aggregate - 11.82%
d. superplasticizer 0.47 e. antifoam agent - 0.01%
f. metallic filler -10/25 mesh stainless steel 34.8%
80/100 mesh stainless steel 18.7%; and g. water - 6.66%.
8. The mixture of Claim 7 in which the Portland cement is API Class H.
9. The mixture of Claim 5 in which the superplasticizer is sodium salt of formaldehyde condensate of naphthalene beta sulfonic acid.
10. The mixture of Claim 5 in which the antifoam agent is Tri-n-butyl phosphate.
11. The mixture of Claim 5 in which the irregularly shaped metallic filler is type 316 stainless steel particles.
12. The mixture of Claim 5 in which the less active siliceous aggregate comprises particles of quartz or silica finer than 5 microns.
13. A method of preparing cast objects of a cementitious composite material with high strength, vacuum integrity and good thermal properties and which are characterized by an absence of a continuous network of interconnected pores which comprises:
a. preparing a blend of Portland cement and fine crystalline silica particles in a mixing vessel b. adding superplasticizer and an antifoam agent to produce a mixture thereof c. adding said mixture to said blend in said vessel, with stirring d. preparing a mixture of at least two different size fractions of stainless steel particles e. mixing said mixture of stainless steel particles into the contents of the mixing vessel and f. casting the resulting material into an object.
14. A cementitious object with high strength, vacuum integrity and good thermal properties prepared by the method of Claim 13.
15. A cementitious object with vacuum integrity produced from the mixture of Claim 5.
CA000457930A 1983-06-30 1984-06-29 Cementitious composite material with metal aggregate Expired CA1220791A (en)

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US509,677 1983-06-30
US06/509,677 US4482385A (en) 1983-06-30 1983-06-30 Cementitious composite material with stainless steel particulate filler

Publications (1)

Publication Number Publication Date
CA1220791A true CA1220791A (en) 1987-04-21

Family

ID=24027646

Family Applications (1)

Application Number Title Priority Date Filing Date
CA000457930A Expired CA1220791A (en) 1983-06-30 1984-06-29 Cementitious composite material with metal aggregate

Country Status (11)

Country Link
US (1) US4482385A (en)
EP (1) EP0149644B1 (en)
JP (1) JPS61502603A (en)
AU (1) AU3107284A (en)
BR (1) BR8406963A (en)
CA (1) CA1220791A (en)
DE (1) DE3475778D1 (en)
IL (1) IL72230A (en)
IT (1) IT1214472B (en)
WO (1) WO1985000358A1 (en)
ZA (1) ZA844883B (en)

Families Citing this family (26)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB8421605D0 (en) * 1984-08-24 1984-09-26 Marley Roof Tile Lightweight concrete roof tiles
US4599211A (en) * 1984-11-21 1986-07-08 Research One Limited Partnership Thermal treatment of concretes containing stainless steel
US4891071A (en) * 1984-11-21 1990-01-02 Cemcom Corporation Cementitious composite material with vacuum integrity at elevated temperatures
US4584327A (en) * 1985-05-24 1986-04-22 Halliburton Company Environmentally compatable high density drilling mud, cement composition or blow-out fluid
JPS6217056A (en) * 1985-07-12 1987-01-26 清水建設株式会社 High fluidity concrete
US4666520A (en) * 1985-09-18 1987-05-19 F. P. C. Research, Inc. Cementitious composite material with silicon carbide aggregate
IT1200142B (en) * 1985-11-08 1989-01-05 Modern Advanced Concrete METHOD TO IMPROVE THE FLUIDIFICATION OF CEMENT MIXTURES
AT385028B (en) * 1986-06-02 1988-02-10 Eternit Werke Hatschek L MIXTURE FOR PRODUCING TIED FIBER-BASED MOLDED BODIES BY THE WET METHOD
US4792361A (en) * 1986-08-08 1988-12-20 Cemcom Corp. Cementitious composite friction compositions
US4780141A (en) * 1986-08-08 1988-10-25 Cemcom Corporation Cementitious composite material containing metal fiber
EP0287918A1 (en) * 1987-04-13 1988-10-26 Cemcom Corporation Chemically bonded ceramic armor materials
IL86829A0 (en) * 1987-07-13 1988-11-30 Cemcom Corp Chemically bonded ceramic armor materials
NL8801241A (en) * 1988-05-11 1989-12-01 Stamicarbon DIE AND METHOD FOR MANUFACTURING SUCH A DIE.
US4936939A (en) * 1989-05-05 1990-06-26 Ceracom Technologies, Inc. Fabric-reinforced ceramic matrix composite material
DE59109055D1 (en) * 1991-06-11 1998-10-22 Frank Gmbh & Co Kg Max Cement-bound building material
FR2708263B1 (en) * 1993-07-01 1995-10-20 Bouygues Sa Composition of metal fiber concrete for molding a concrete element, elements obtained and thermal cure process.
US5531823A (en) * 1995-02-06 1996-07-02 Atomic Energy Of Canada Limited Low-heat high-performance concrete
US5890840A (en) * 1995-12-08 1999-04-06 Carter, Jr.; Ernest E. In situ construction of containment vault under a radioactive or hazardous waste site
TR199802083T2 (en) * 1996-04-18 1998-12-21 Concrete Technology 1, Ltd. Fibre-reinforced concrete building material.
FR2778654B1 (en) 1998-05-14 2000-11-17 Bouygues Sa CONCRETE COMPRISING ORGANIC FIBERS DISPERSED IN A CEMENTITIOUS MATRIX, CONCRETE CEMENTITIOUS MATRIX AND PREMIXES
FR2859722B1 (en) * 2003-09-15 2006-02-03 Wheelabrator Allevard ABRASION RESISTANT COMPOSITE MATERIAL COMPRISING THE STEEL-BASED GRILLEILLE AND METHOD FOR MANUFACTURING SUCH MATERIAL
CL2009000372A1 (en) * 2008-03-03 2009-11-13 United States Gypsum Co Fiber-reinforced armored cementitious panel, comprising a cured phase cementitious core made up of inorganic cement, inorganic mineral, pozzolanic filler, polycarboxylate and water, and a coating layer bonded to a surface of the cured phase.
CL2009000373A1 (en) * 2008-03-03 2009-10-30 United States Gypsum Co Method to make an explosive resistant panel, with the steps of preparing an aqueous cementitious mixture of cement, inorganic fillers and pozzolanic, polycarboxylate self-leveling agent, and forming the mixture into a panel with fiber reinforcement, then curing, polishing, cutting and cure the panel.
US8061257B2 (en) * 2008-03-03 2011-11-22 United States Gypsum Company Cement based armor panel system
CL2009000371A1 (en) * 2008-03-03 2009-10-30 United States Gypsum Co Cementitious composition, containing a continuous phase that results from the curing of a cementitious mixture, in the absence of silica flour, and comprising inorganic cement, inorganic mineral, pozzolanic filler, polycarboxylate and water; and use of the composition in a cementitious panel and barrier.
ITMI20130998A1 (en) * 2013-06-17 2014-12-18 Freni Brembo Spa FRICTION MATERIAL FOR BRAKING PADS AND RELATIVE BRAKING PADS

Family Cites Families (15)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
US4038444A (en) * 1972-04-05 1977-07-26 Erwin Steinhauser Method of producing a metallic plating
JPS5328175B2 (en) * 1973-12-04 1978-08-12
SE7414809L (en) * 1974-11-26 1976-05-28 Skf Nova Ab CONCRETE REQUIREMENTS AND METHODS OF MANUFACTURE
US4310486A (en) * 1976-01-16 1982-01-12 Cornwell Charles E Compositions of cementitious mortar, grout and concrete
JPS52126418A (en) * 1976-04-16 1977-10-24 Kiyoshi Hayashi Flat concrete boards
RO72773B (en) * 1976-07-09 1984-03-31 Aksjeselskapet Norcem Process for preparing non-corrodible concrete compositions
JPS5360932A (en) * 1976-11-15 1978-05-31 Mitsubishi Heavy Ind Ltd Metallic particle concrete
JPS5369223A (en) * 1976-12-01 1978-06-20 Toyoshige Teranishi Prevention of cracking in concrete and mortar and aggregate increases strength
JPS5516768A (en) * 1978-07-25 1980-02-05 Furukawa Battery Co Ltd:The Method and device for simultaneous multiple casting
NO163449C (en) * 1978-11-03 1996-11-25 Aalborg Portland Cement Method of making a shaped article
US4255195A (en) * 1979-03-26 1981-03-10 Hoelter H Compositions containing silicon dioxide
JPS6019983B2 (en) * 1980-06-04 1985-05-18 東洋製罐株式会社 Inner container loading/unloading device for outer container of flexible packaging carrier
JPS57156362A (en) * 1981-03-23 1982-09-27 Kawasaki Steel Co Steel fiber and manufacture
JPS5836982A (en) * 1981-08-15 1983-03-04 黒崎窯業株式会社 Volume-stable heat resistant composition and premold product therefrom
JPS5874561A (en) * 1981-10-23 1983-05-06 株式会社 イシマル Artificial stone and manufacture

Also Published As

Publication number Publication date
EP0149644A1 (en) 1985-07-31
IT8421683A0 (en) 1984-06-29
EP0149644A4 (en) 1985-11-21
BR8406963A (en) 1985-06-11
EP0149644B1 (en) 1988-12-28
DE3475778D1 (en) 1989-02-02
WO1985000358A1 (en) 1985-01-31
JPS61502603A (en) 1986-11-13
IT1214472B (en) 1990-01-18
IL72230A0 (en) 1984-10-31
US4482385A (en) 1984-11-13
ZA844883B (en) 1986-05-28
IL72230A (en) 1987-12-31
AU3107284A (en) 1985-02-07

Similar Documents

Publication Publication Date Title
CA1220791A (en) Cementitious composite material with metal aggregate
US4780141A (en) Cementitious composite material containing metal fiber
US5595597A (en) Process for producing phosphomagnesia cements having reduced sensitivity to water
Patankar et al. Effect of concentration of sodium hydroxide and degree of heat curing on fly ash-based geopolymer mortar
Sharifi et al. Recycled glass replacement as fine aggregate in self-compacting concrete
EP0088587B1 (en) Hydraulic cement composition
Yu et al. Effect of seawater for mixing on properties of potassium magnesium phosphate cement paste
US2547127A (en) Calcium silicate of microcrystalline lathlike structure
US5531823A (en) Low-heat high-performance concrete
PL180782B1 (en) Aerogel containing laminar material, method of obtaining same and application thereof
US4412863A (en) Inorganic cement compositions having controlled thermal expansion coefficients
US4505753A (en) Cementitious composite material
US2914413A (en) Cement composition and method of preparation
Xu et al. Evaluation of inherent factors on flowability, cohesiveness and strength of cementitious mortar in presence of zeolite powder
EP1888480B1 (en) High performance concrete with a quick resistance development lacking added materials with latent hydraulic activity
Zuda et al. Effect of high temperatures on the properties of alkali activated aluminosilicate with electrical porcelain filler
Abdel-Jawad et al. The combined effect of water and temperature on the strength of sulfur concrete
US3116158A (en) Thermal insulating materials and method of making
US9957197B1 (en) Porous geopolymers
US3607325A (en) Refractory-ceramic composition and method
CN115215606A (en) Mortar suitable for negative temperature environment and preparation method thereof
Salim et al. Microstructure, strength, and physical properties of metakaolin-based geopolymer mortar
US3207612A (en) Thixotropic composition
JPS585860B2 (en) Method for manufacturing acid-resistant cement
RU2040503C1 (en) Building mixture

Legal Events

Date Code Title Description
MKEX Expiry